Systematic-Review-Drug-Efficiency-Dissertation-Sample-Work-Tutors-India
Idiopathic Pulmonary Fibrosis (IPF) as the name suggests is a progressive disorder with no known aetiology. It is characterised by the thickening of the alveoli due to scarring resulting in cough. It is known to primarily occur in older adults over 60 years of age. The findings of IPF have a known association of Usual Interstitial Pneumonia (UIP) (Raghu et al., 2011; Kawano-Dourado & Kairalla, 2013; Wells, 2013). It has been deemed that the prognosis is generally poor when UIP has been confirmed (King et al., 2001b). The median survival rate of IPF is 50%, typically around two years after diagnosis (Raghu et al., 2011; King et al., 2001b). Idiopathic Pulmonary Fibrosis (IPF) as the name suggests is a progressive disorder with no known aetiology. It is characterised by the thickening of the alveoli due to scarring resulting in cough. It is known to primarily occur in older adults over 60 years of age. The findings of IPF have a known association of Usual Interstitial Pneumonia (UIP) (Raghu et al., 2011; Kawano-Dourado & Kairalla, 2013; Wells, 2013). It has been deemed that the prognosis is generally poor when UIP has been confirmed (King et al., 2001b). The median survival rate of IPF is 50%, typically around two years after diagnosis (Raghu et al., 2011; King et al., 2001b).
ole remains uncertain as anti-interleukin-5 only partially depletes numbers in asthmatic airway. American journal of respiratory and critical care medicine. 167 (2). pp. 199– 204. Fulmer, J.D., Roberts, W.C., von Gal, E.R. & Crystal, R.G. (1979). Morphologic-physiologic correlates of the severity of fibrosis and degree of cellularity in idiopathic pulmonary fibrosis. Journal of Clinical Investigation. [Online]. 63 (4). pp. 665–676. Available from: http://www.jci.org/articles/view/109349. Gaede, K.I., Mamat, U. & Müller-Quernheim, J. (2004). Differential gene expression pattern in alveolar macrophages of patients with sarcoidosis and tuberculosis. Journal of molecular medicine (Berlin, Germany). 82 (3). pp. 206–210. García-Sancho, C., Buendía-Roldán, I., Fernández-Plata, M.R., Navarro, C., Pérez-Padilla, R., Vargas, M.H., Loyd, J.E. & Selman, M. (2011). Familial pulmonary fibrosis is the strongest risk factor for idiopathic pulmonary fibrosis. Respiratory medicine. [Online]. 105 (12). pp. 1902–7. Available from: http://www.ncbi.nlm.nih.gov/pubmed/21917441. George, T.J. (2011). Lung Transplant in Idiopathic Pulmonary Fibrosis. Archives of Surgery. [Online]. 146 (10). pp. 1204–1209. Available from: http://archsurg.jamanetwork.com/article.aspx?doi=10.1001/archsurg.2011.239. Ghafoori, P., Marks, L.B., Vujaskovic, Z. & Kelsey, C.R. (2008). Radiation-induced lung injury. Assessment, management, and prevention. Oncology (Williston Park, N.Y.). 22 (1). pp. 37-47–3. Giotopoulos, G., Symonds, R.P., Foweraker, K., Griffin, M., Peat, I., Osman, A. & Plumb, M. (2007). The late radiotherapy normal tissue injury phenotypes of telangiectasia, fibrosis and atrophy in breast cancer patients have distinct genotype-dependent causes. British journal of cancer. 96 (6). pp. 1001–1007. Giri, S.N., Hyde, D.M. & Hollinger, M.A. (1993). Effect of antibody to transforming growth factor beta on bleomycin induced accumulation of lung collagen in mice. Thorax. 48 (10). pp. 959–966. Giri, S.N., Leonard, S., Shi, X., Margolin, S.B. & Vallyathan, V. (1999). Effects of © 2017-2018 All Rights Reserved, No part of this document should be modified/used without prior consent Tutors India - Your trusted mentor since 2001 www.tutorindia.com I UK # +44-1143520021, info@tutorsindia.com Page 126 of 172
pirfenidone on the generation of reactive oxygen species in vitro. Journal of environmental pathology, toxicology and oncology : official organ of the International Society for Environmental Toxicology and Cancer. [Online]. 18 (3). pp. 169–77. Available from: http://www.ncbi.nlm.nih.gov/pubmed/15281229. Greene, K.E., Wright, J.R., Steinberg, K.P., Ruzinski, J.T., Caldwell, E., Wong, W.B., Hull, W., Whitsett, J.A., Akino, T., Kuroki, Y., Nagae, H., Hudson, L.D. & Martin, T.R. (1999). Serial changes in surfactant-associated proteins in lung and serum before and after onset of ARDS. American journal of respiratory and critical care medicine. [Online]. 160 (6). pp. 1843–50. Available from: http://www.ncbi.nlm.nih.gov/pubmed/10588595. Gribbin, J., Hubbard, R.B., Le Jeune, I., Smith, C.J.P., West, J. & Tata, L.J. (2006). Incidence and mortality of idiopathic pulmonary fibrosis and sarcoidosis in the UK. Thorax. [Online]. 61 (11). pp. 980–5. Available from: http://www.ncbi.nlm.nih.gov/pubmed/16844727. Grubstein, A., Bendayan, D., Schactman, I., Cohen, M., Shitrit, D. & Kramer, M.R. (2005). Concomitant upper-lobe bullous emphysema, lower-lobe interstitial fibrosis and pulmonary hypertension in heavy smokers: report of eight cases and review of the literature. Respiratory medicine. [Online]. 99 (8). pp. 948–54. Available from: http://www.ncbi.nlm.nih.gov/pubmed/15950135. Gulack, B.C., Ganapathi, A.M., Speicher, P.J., Meza, J.M., Hirji, S.A., Snyder, L.D., Davis, R.D. & Hartwig, M.G. (2015). What Is the Optimal Transplant for Older Patients With Idiopathic Pulmonary Fibrosis? The Annals of Thoracic Surgery. [Online]. 100 (5). pp. 1826–1833. Available from: http://linkinghub.elsevier.com/retrieve/pii/S0003497515008279. Gunther, A., Korfei, M., Mahavadi, P., von der Beck, D., Ruppert, C. & Markart, P. (2012). Unravelling the progressive pathophysiology of idiopathic pulmonary fibrosis. European Respiratory Review. [Online]. 21 (124). pp. 152–160. Available from: http://err.ersjournals.com/cgi/doi/10.1183/09059180.00001012. Gustafson, T., Dahlman-Höglund, A., Nilsson, K., Ström, K., Tornling, G. & Torén, K. © 2017-2018 All Rights Reserved, No part of this document should be modified/used without prior consent Tutors India - Your trusted mentor since 2001 www.tutorindia.com I UK # +44-1143520021, info@tutorsindia.com Page 127 of 172
- Page 97: oom air 3 Sakamoto et al 15 Effecti
- Page 101 and 102: Of the studies considered for the s
- Page 103: 4.6 Evaluation of Efficacy of Prife
- Page 107: change in the lowest SPO2 during th
- Page 111: PaO2, and SaO2; episodes of AE-IPF
- Page 115 and 116: The efficacy of using NAC in combin
- Page 117 and 118: group. It is revealed that at the 2
- Page 119 and 120: CHAPTER V: DISCUSSION AND CONCLUSIO
- Page 121 and 122: contradicting results 50 51 . A res
- Page 123 and 124: tolerability and safety of pirfenid
- Page 125 and 126: equired. An exploratory efficacy an
- Page 127 and 128: as to verify the results and acquir
- Page 129 and 130: © 2017-2018 All Rights Reserved, N
- Page 131 and 132: American Thoracic Society. Idiopath
- Page 133 and 134: and clinical immunology. 115 (1). p
- Page 135 and 136: Behr, J., Maier, K., Degenkolb, B.,
- Page 137 and 138: Bowling, A. (2009). Research Method
- Page 139 and 140: 878-81. Available from: http://www.
- Page 141 and 142: http://www.ncbi.nlm.nih.gov/pubmed/
- Page 143 and 144: El-Chemaly, S., Ziegler, S.G., Cala
- Page 145: Flaherty, K.R., Andrei, A.-C., Murr
- Page 149 and 150: Hansell, D.M., Bankier, A.A., MacMa
- Page 151 and 152: proteoglycan deposition in the airw
- Page 153 and 154: Nishimura, J. & Inoue, T. (2009). A
- Page 155 and 156: 313-9. Available from: http://www.n
- Page 157 and 158: Pereira, C.A., Sahn, S.A., Sussman,
- Page 159 and 160: interstitial pneumonia: the prognos
- Page 161 and 162: Leslie, K.O., Gruden, J.F., Parish,
- Page 163 and 164: America. 25 (4). pp. 709-721. Marti
- Page 165 and 166: Meyer, A., Buhl, R. & Magnussen, H.
- Page 167 and 168: Moseley, P.L., Hemken, C. & Hunning
- Page 169 and 170: topics/topics/idiopathic-pulmonary-
- Page 171 and 172: Olson, A.L., Swigris, J.J., Lezotte
- Page 173 and 174: Piguet, P.F., Vesin, C., Grau, G.E.
- Page 175 and 176: open-label Phase II study. American
- Page 177 and 178: Rødningen, O.K., Børresen-Dale, A
- Page 179 and 180: Experimental Biology and Medicine.
- Page 181 and 182: Silva, C.I.S., Müller, N.L., Fujim
- Page 183 and 184: Sutton, A.J. (2000). Methods for me
- Page 185 and 186: (11). pp. 1085-1094. Tomioka, H., K
- Page 187 and 188: Wang, Q., Zhu, H., Zhou, W.-G., Guo
- Page 189 and 190: http://www.nature.com/doifinder/10.
- Page 191 and 192: silica-induced lung fibrosis in the
pirfenidone on the generation of reactive oxygen<br />
species in vitro. Journal of<br />
environmental pathology, toxicology and oncology : official organ of the International<br />
Society for Environmental Toxicology and Cancer. [Online]. 18 (3). pp. 169–77.<br />
Available from: http://www.ncbi.nlm.nih.gov/pubmed/15281229.<br />
Greene, K.E., Wright, J.R., Steinberg, K.P., Ruzinski, J.T., Caldwell, E., Wong, W.B., Hull,<br />
W., Whitsett, J.A., Akino, T., Kuroki, Y., Nagae, H., Hudson, L.D. & Martin, T.R.<br />
(1999). Serial changes in surfactant-associated proteins in lung and serum before and<br />
after onset of ARDS. American journal of respiratory and critical care medicine.<br />
[Online]. 160 (6). pp. 1843–50. Available from:<br />
http://www.ncbi.nlm.nih.gov/pubmed/10588595.<br />
Gribbin, J., Hubbard, R.B., Le Jeune, I., Smith, C.J.P., West, J. & Tata, L.J. (2006). Incidence<br />
and mortality of idiopathic pulmonary fibrosis and sarcoidosis in the UK. Thorax.<br />
[Online]. 61 (11). pp. 980–5. Available from:<br />
http://www.ncbi.nlm.nih.gov/pubmed/16844727.<br />
Grubstein, A., Bendayan, D., Schactman, I., Cohen, M., Shitrit, D. & Kramer, M.R. (2005).<br />
Concomitant upper-lobe bullous emphysema, lower-lobe interstitial fibrosis and<br />
pulmonary hypertension in heavy smokers: report of eight cases and review of the<br />
literature. Respiratory medicine. [Online]. 99 (8). pp. 948–54. Available from:<br />
http://www.ncbi.nlm.nih.gov/pubmed/15950135.<br />
Gulack, B.C., Ganapathi, A.M., Speicher, P.J., Meza, J.M., Hirji, S.A., Snyder, L.D., Davis,<br />
R.D. & Hartwig, M.G. (2015). What Is the Optimal Transplant for Older Patients With<br />
Idiopathic Pulmonary Fibrosis? The Annals of Thoracic Surgery. [Online]. 100 (5). pp.<br />
1826–1833. Available from:<br />
http://linkinghub.elsevier.com/retrieve/pii/S0003497515008279.<br />
Gunther, A., Korfei, M., Mahavadi, P., von der Beck, D., Ruppert, C. & Markart, P. (2012).<br />
Unravelling the progressive pathophysiology of idiopathic pulmonary fibrosis.<br />
European Respiratory <strong>Review</strong>. [Online]. 21 (124). pp. 152–160. Available from:<br />
http://err.ersjournals.com/cgi/doi/10.1183/09059180.00001012.<br />
Gustafson, T., Dahlman-Höglund, A., Nilsson, K., Ström, K., Tornling, G. & Torén, K.<br />
© 2017-2018 All Rights Reserved, No part of this document should be modified/used without prior consent<br />
<strong>Tutors</strong> <strong>India</strong> - Your trusted mentor since 2001<br />
www.tutorindia.com I UK # +44-1143520021, info@tutorsindia.com<br />
Page 127 of 172